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poruchy močovinového cyklu, vrodené

Subject h.	poruchy močovinového cyklu, vrodené
Subject h.	Urea Cycle Disorders, Inborn
Entry terms	poruchy cyklu kyseliny močovej, vrodené poruchy močovinového cyklu porucha močovinového cyklu, vrodená
English X references	Inborn Urea Cycle Disorder Urea Cycle Disorders
Scope note in English	Rare congenital metabolism disorders of the urea cycle. The disorders are due to mutations that result in complete (neonatal onset) or partial (childhood or adult onset) inactivity of an enzyme, involved in the urea cycle. Neonatal onset results in clinical features that include irritability, vomiting, lethargy, seizures, NEONATAL HYPOTONIA; RESPIRATORY ALKALOSIS; HYPERAMMONEMIA; coma, and death. Survivors of the neonatal onset and childhood/adult onset disorders share common risks for ENCEPHALOPATHIES, METABOLIC, INBORN; and RESPIRATORY ALKALOSIS due to HYPERAMMONEMIA.
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